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Fig. 2 | BMC Bioinformatics

Fig. 2

From: Learning mutational graphs of individual tumour evolution from single-cell and multi-region sequencing data

Fig. 2

aTRaIT processes a binary matrix D that stores the presence or absence of a variable in a sample (e.g., a mutation, a CNA, or a persistent epigenetic states). b.TRaIT merges the events occurring in the same samples (x1, x2 and x4, merged to A), as the statistical signal for their temporal ordering is undistinguishable. The final model include such aggregate events. c. We estimate via bootstrap the prima facie ordering relation that satisfies Suppes’ conditions (Eq. 1) for statistical association. This induces a graph GPF over variables xi, which is weighted by information-theoretic measures for variables’ association such as mutual information or pointwise mutual information. dTRaIT employs heuristic strategies to remove loops from GPF and produce a new graph GNL [14]. eEdmonds’s algorithm can be used to reconstruct the optimal minimum spanning tree GMO that minimises the weights in GNL; here we use point-wise mutual information (pmi). f.Chow-Liu is a Bayesian mode-selection strategy that computes an undirected tree as a model of a joint distribution on the annotated variable. Then, we provide edge direction (temporal priority), with Suppes’ condition (Eq. 1) on marginal probabilities. Therefore, confluences are possible in the output model GMO in certain conditions

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